EasyManua.ls Logo

St. Jude Medical CD3357-40C User Manual

St. Jude Medical CD3357-40C
34 pages
To Next Page IconTo Next Page
To Next Page IconTo Next Page
Page #1 background imageLoading...
Page #1 background image
Ellipse™
Fortify Assura™
Tiered-therapy Cardioverter/Defibrillator
Quadra Assura™, Quadra Assura MP™
Unify Assura
Cardiac Resynchronization Device, Tiered-therapy Cardioverter/Defibrillator
Question and Answer IconNeed help?

Do you have a question about the St. Jude Medical CD3357-40C and is the answer not in the manual?

St. Jude Medical CD3357-40C Specifications

General IconGeneral
BrandSt. Jude Medical
ModelCD3357-40C
CategoryMedical Equipment
LanguageEnglish

Summary

Indications and Usage

AF Suppression Pacing

Pacing for suppression of paroxysmal or persistent atrial fibrillation in patients with ICD indication and sinus node dysfunction.

ICD/CRT-D for Heart Failure

ICD/CRT-D for reducing heart failure symptoms in specific patient populations with low ejection fraction.

ICD/CRT-D for AV Nodal Ablation Patients

ICD/CRT-D for maintaining ventricular synchrony in patients post AV nodal ablation with heart failure.

MR Conditional System

Contraindications

Warnings and Precautions

Resuscitation Availability

Ensure external defibrillator and skilled personnel are available during device testing.

Lead System Compatibility

Do not use incompatible lead systems to avoid undersensing or therapy failure.

Handling Precautions (Shock Hazard)

Disable therapy or program OFF during handling to prevent shock from charged device.

Magnetic Resonance Imaging (MRI)

Sterilization, Storage and Handling

Device Implant Restrictions

Do not implant if dropped, package damaged, or after use-before date.

Follow-up Testing

Post-Implant Testing Requirements

Ensure external defibrillator and skilled personnel are present during post-implant testing.

Implantation and Device Programming

Magnet Use During Implantation

Do not position a magnet over the device as it suspends detection and treatment.

Device Replacement and Implant Depth

Replace device at ERI. Implant no deeper than 5 cm and avoid close proximity to bone.

Pulse Generator Explant and Disposal

Explant and Disposal Procedures

Interrogate device, turn off therapies, return explanted devices, do not incinerate.

Environmental and Medical Therapy Hazards

External Defibrillation Precautions

Paddle Placement and Energy Use

Position paddles away from device (min 13 cm) and use lowest energy output. Confirm function after.

Specific Therapy Hazards

Therapeutic Stimulation Hazards

Potential Adverse Events

Physician Training Requirements

Maintaining Device Effectiveness

Device Handling and Information

Technical Support Contacts

Related product manuals